MDS Pharma Services offers a fully flexible range of medical and scientific writing services.
Our medical writers can provide a stand-alone service, collaborating with our client's
project team to write or review a clinical study report, protocol, patient safety
narratives, manuscript for publication, or periodic safety update report. Our resources
can be utilized as part of a full service project, and assist in the regulatory
submission process with integrated summaries of safety, integrated summaries of
efficacy and electronic regulatory submissions.
MDS Pharma Services' medical writing team follows our global standard operating procedures
(SOPs) to ensure that protocol and clinical study report development are performed in a
consistent manner throughout the company. SOPs and templates provided by the client to
our team of medical writers would supersede those of MDS Pharma Services. The requisite
International Conference of Harmonisation's (ICH) guidelines are also utilized to ensure
that the document provided meets the standards required for regulatory submission.
Our team of medical writers based in France, Spain, UK and USA is dedicated to delivering high
quality output, with full documentation and review at all stages. With proactive input,
ongoing involvement and effective communication throughout the project, the medical
writing department at MDS Pharma Services will provide timeliness, accuracy and integrity
to your clinical programs.
